首页> 外文期刊>Romanian Journal of Morphology and Embryology >Cytoarchitecture of steroid dependent target tissues after testosterone administration compared to nandrolone decanoate in castrated rats in the aim of Hershberger bio test
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Cytoarchitecture of steroid dependent target tissues after testosterone administration compared to nandrolone decanoate in castrated rats in the aim of Hershberger bio test

机译:为了进行Hershberger生物测试,在去势大鼠中,睾丸激素给药后与癸酸诺龙相比,甾体依赖性靶组织的细胞结构

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The objective was the cytoarchitecture evaluation of known steroid dependent target tissues after administering of testosterone, compared to action of its more active ester, nortestosterone (nandrolone decanoate) in castrated rat males in the aim of Hershberger bio test. Study was performed on 30 castrated male Wistar rats, aged between 35 and 39 days, in peripubertal period, divided into five groups. Androgen doses administration begun at the rats age of 49 days. Animals were injected i.m., daily, for 10 consecutive days as follows: Aquatest (Balkan Pharmaceuticals Ltd., Moldova) testosterone aqueous solution: Testosterone I group (0.4 mg/animal); Testosterone II (0.8 mg/animal); (Deca-Durabolin, Balkan Pharmaceuticals); nandrolone decanoate oily solution: Nortestosterone I (1.5 mg/kg body weight); Nortestosterone II (7.5 mg/kg body weight) and Control (White sesame oil, Manicos, Romania, 0.1 mL/animal). Gonadectomy (GDX) induced modifications of target tissues wet weight accompanied by important modifications in cytoarchitecture. Changes following exogenous administration of testosterone and nortestosterone decanoate were found in: liver (granular dystrophy, mega-mitochondria, tubular intumescences), prostate (increasing of the structural elements), seminal vesicles (hyalinosis, thickening of cell walls and the hyaline presence), levator ani-bulbo-cavernosus muscle (muscle fibbers dilacerations), bulbourethral glands (muscular fibbers rarefaction by fluid accumulation) demonstrating the disruptor activity especially for overdosed nandrolone decanoate.
机译:目的是在进行睾丸激素治疗后,对已知的类固醇依赖性靶组织进行细胞结构评估,与其更活性的酯,睾丸激素去甲睾酮(癸酸诺龙)的作用相比,是为了进行赫什伯格生物试验。在青春期将30只年龄在35至39天之间的pub割雄性Wistar大鼠进行了研究,分为五组。雄激素剂量的给药始于49天大的大鼠。每天每天如下连续10天每天给动物注射:Aquatest(摩尔多瓦Balkan Pharmaceuticals Ltd.)睾丸素水溶液:睾丸素I组(0.4 mg /动物);睾丸激素II(0.8毫克/动物); (Deca-Durabolin,巴尔干制药);癸酸诺龙酮油溶液:去甲睾酮I(1.5 mg / kg体重);去甲睾酮II(7.5 mg / kg体重)和对照(白麻油,Manicos,罗马尼亚,0.1 mL /动物)。角膜切除术(GDX)诱导目标组织湿重的改变,伴随着细胞结构的重要改变。外源性施用睾丸激素和癸酸癸酸睾丸激素后发现以下变化:肝脏(颗粒性营养不良,巨线粒体,肾小管膨胀),前列腺(结构元素增加),精囊(透明质酸,细胞壁增厚和透明质存在),提肛肌,肾上腺-海绵体肌肉(肌纤维扩张),球脑管腺体(由于积聚的肌纤维稀疏)证明了破坏活性,特别是对于癸酸诺龙的给药。

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